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A study of effectiveness of Remimazolam in Modified Electroconvulsive Therapy

A study of effectiveness of Remimazolam in Modified Electroconvulsive Therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1030240216
Enrollment
60
Registered
2024-07-12
Start date
2024-07-12
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Drug-resistant depression Schizophrenia

Interventions

Patients will be randomly assigned to remimazolam besilate or propofol groups, each receiving the two drugs at the time of mECT treatment. Delirium will be assessed with the 4AT-J before and after tre

Sponsors

Shimono Shinako
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients admitted to the Mental Care Center Ward of Showa University Northern Yokohama Hospital and undergoing mECT 2)Patients with ASA-PS2 and 3 3)Persons who have obtained written consent to participate in this study from the individual or a surrogate 4)Those who are judged to be eligible for participation in this study by the physician in charge of the study, etc. in the pre-test specified in the protocol of this study

Exclusion criteria

Exclusion criteria: 1) Patients with intracranial hypertension, cerebral aneurysm, recent myocardial infarction (within 3 months), angina pectoris, congestive heart failure 2) Patients with bronchial asthma 3) Patients with neuromuscular disease 4) Patients with a history of hypersensitivity to remimazolam besilate, propofol itself or its components, acute angle closure glaucoma, myasthenia gravis, shock, coma, or acute alcohol intoxication with suppressed vital signs 5) Patients within 3 months of participation in other clinical research 6) Other patients who are judged by the investigator to be ineligible for this study.

Design outcomes

Primary

MeasureTime frame
4AT-J(Immediately after surgery)

Secondary

MeasureTime frame
Induction time, hemodynamic changes, seizure duration, recovery time, incidence of vomiting reflex, cough, and tears during anesthesia induction 4AT-J (morning of treatment day, 1 hour after treatment, 3 hours after treatment, morning of next day after treatment)

Contacts

Public ContactShinako Shimono

SHOWA University Northern Yokohama Hospital

v4nako@dent.showa-u.ac.jp+81-45-949-7000

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026